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Hydrogenation of aromatic ligands during the synthesis of π-arene-π-cyclopentadienyliron mono- and dications. Evidence from 1H and 13C magnetic resonance studies by R.G. Sutherland; S.C. Chen; J. Pannekoek; C.C. Lee is a Chemistry article available to read on EtoBox.
What is Hydrogenation of aromatic ligands during the synthesis of π-arene-π-cyclopentadienyliron mono- and dications. Evidence from 1H and 13C magnetic resonance studies about?
Anthracene reacts with,-ferrocene in the presence of AlClJAl to form the same mono-and dications derived from 9,10-dihydroanthracene. Naphthalene yields arene complexes of both naphthalene and tetralin, the product formed being dependent on the reaction temperature. ~-. .
Who reads Hydrogenation of aromatic ligands during the synthesis of π-arene-π-cyclopentadienyliron mono- and dications. Evidence from 1H and 13C magnetic resonance studies?
It is typically read by researchers, students, and practitioners in Chemistry.
- Author
- R.G. Sutherland; S.C. Chen; J. Pannekoek; C.C. Lee
- Publisher
- Elsevier Science; Elsevier ; Elsevier BV (ISSN 0022-328X)
- Published
- 1975
- Language
- EN
- Field
- Chemistry (Physical Sciences)
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